Product Details

SNP ID

rs6000172

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36191154 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGCTCCTGAGCCCACTGCCTCAGC[A/G]ACTCAGCAGACTCGGATTTTGCCCC

Phenotype

MIM: 607254

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

APOL4 PubMed Links

Additional Information

For this assay, SNP(s) [rs111781032] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

APOL4

Gene Name

apolipoprotein L4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030643.4	1391	Missense Mutation	TCG,TTG	S323L	NP_085146.2
NM_145660.2	1391	Missense Mutation	TCG,TTG	S326L	NP_663693.1

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